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Wanshimac comprehensive diagnosis and treatment instrument - Taiwan Registration 60806c957f98ad85a72cc5437dd40fce

Access comprehensive regulatory information for Wanshimac comprehensive diagnosis and treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60806c957f98ad85a72cc5437dd40fce and manufactured by SHINE ALPHA ELECTRONIC CO., LTD.. The authorized representative in Taiwan is SHINE ALPHA ELECTRONIC CO., LTD..

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60806c957f98ad85a72cc5437dd40fce
Registration Details
Taiwan FDA Registration: 60806c957f98ad85a72cc5437dd40fce
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Device Details

Wanshimac comprehensive diagnosis and treatment instrument
TW: ่ฌ้ฉ็พŽ็ถœๅˆ่จบ็™‚ๅ„€
Risk Class 2

Registration Details

60806c957f98ad85a72cc5437dd40fce

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order. For details, such as the approved copy of the Chinese imitation order (the original approval of the 101.05.04 approved copy of the imitation order and the approved label will be recycled and invalidated)

H Gastroenterology and urology

H.5320 ้žๆคๅ…ฅๅผ้›ปๅญๆŽ’ๅฐฟ่‡ชๅˆถ่ฃ็ฝฎ

Domestic

Dates and Status

Jan 28, 2012

Jan 28, 2027